Novel Support Surface to Alleviate Pressure Ulcer

Not Applicable

Completed

• Conditions: Pressure Injury; Immobility Syndrome; Pressure Ulcer

• Registration Number: NCT04251897
• Lead Sponsor: Tan Tock Seng Hospital

Brief Summary

A prototype support surface has been designed which aims to successfully redistributes the pressures exerted and provides sufficient support to human soft tissue

We want to prove the effectiveness of the prototype support surface by enlisting patients in a clinical trial, where we will assess the presence of pressure ulcers, and the ability of the patients to tolerate the support surface, and also measure the pressure over time and compare them to when the patients are using standard mattresses.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2020-01-29
• Study First Submitted QC: 2020-01-30
• Study First Posted: 2020-02-05
• Study Start: 2020-09-02
• Primary Completion: 2021-08-30
• Study Completion: 2021-08-30
• Status Verified: 2022-04
• Last Update Submitted: 2022-04-26
• Last Update Posted: 2022-04-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

1. Patients must be immobile as assessed on the braden scale.
2. Patients must require 2 hourly turning
3. Age 21-85

Exclusion Criteria

1. No existing pressure ulcers
2. No active infections, fever, or medical conditions that require constant medical attention.
3. They must also not have severe incontinence requiring the change of diapers more frequently than 4 hours
4. No significant cognitive impairment
5. Pregnant women will be excluded from the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Primary Outcome Measures

Name	Time	Method
PTAUC	For a maximum of 14 days (duration of trial)	pressure-time area under curve
Pressure sores - NPUAP (National Pressure Ulcer Advisory Panel) grade	For a maximum of 14 days (duration of trial)	If pressure sores are present, they will be graded based on the NPUAP grade from 1-4. Location will also be recorded.

Secondary Outcome Measures

Name	Time	Method
Patient's comfort	For a maximum of 14 days (duration of trial)	Patient comfort measured on a visual analogue scale (1- 10)
Discomfort or pain	For a maximum of 14 days (duration of trial)	Presence of discomfort or pain at high risk pressure points. This will be asked of patients, and will be scored as yes or no.
Suggestions	For a maximum of 14 days (duration of trial)	This will be a qualitative open-ended question for patient's verbatim report or suggestions

Trial Locations

Locations (1)

Tan Tock Seng Hospital Rehabilitation Centre; 🇸🇬 Singapore, Singapore